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PCGC: Congenital Heart Disease Genetic Network Study

Identifiers: SRA: SRP025159
BioProject: PRJNA183422
dbGaP: phs000571
Study Type: 
Submission: SRA090072
Abstract: Multi-center, prospective observational cohort study of individuals with congenital heart defects (CHD). Phenotypic data and source DNA derived from 10,000 probands, parents, and families of interest are being collected to investigate relationships between genetic factors and phenotypic and clinical outcomes in patients with CHD.

The SRA runs contain human sequence

These data are available through the dbGaP authorized access system.

Related SRA data

14780 (83.7Tbp; 39.6Tb)